{{Rsnum
|rsid=386833847
|Chromosome=8
|position=144514096
|Orientation=minus
|geno1=(-;-)
|geno2=(-;GGAG)
|geno3=(GGAG;GGAG)
|Gene=RECQL4
|Gene_s=RECQL4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=minus
}}{{ClinVar
|ALT=G
|CHROM=8
|CLNACC=RCV000049815.1
|CLNALLE=1
|CLNDBN=Rapadilino syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1849453:266280:3021
|CLNHGVS=NC_000008.10:g.145739480_145739483delCTCC
|CLNSIG=4
|Disease=Rapadilino syndrome
|FwdREF=GGAG
|REF=GCTCC
|RSPOS=145739479
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386833847
|GENEINFO=RECQL4:9401
|GENE_ID=9401
|GENE_NAME=RECQL4
}}{{PMID Auto
|PMID=18716613
|Title=The mutation spectrum in RECQL4 diseases.
|OA=1
}}